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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903573Generated: October 29, 2026

Potassium borohydride → HCID 13892058, compound

https://huagongshe.com/reaction/1903573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium borohydrideHCID 4192641—
ReactantHCID 70454231HCID 70454231—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 13892058HCID 13892058—

Reaction Steps

While cooling with ice, a solution of 5.4 g (100 mmols) of potassium borohydride in 50 ml of dimethyl formamide is added over 1 hour to a solution of 11.4 g (20 mmols) of 7β-phenoxyacetylamino-3-pyrrolidino-3-cephem-4-carboxylic acid benzhydryl ester in 50 ml of methylene chloride, 50 ml of ethanol and 50 ml of glacial acetic acid. The mixture is then stirred for 36 hours at room temperature, concentrated to half its volume, diluted with ice-water, and extracted several times with methylene chloride. The solvent is then removed by vacuum distillation, affording 7β-phenoxyacetylamino-3-cephem-4-carboxylic acid benzhydryl ester as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436903
Source datasetuspto-grants-1984_03
ORD IDord-706c4a50858140c599b34ba9a6fefacc
Source noteuspto-grants-1984_03